Texas recalls
3,648 federal recalls affecting Texas in the last 12 months - 436 Texas-specific plus 3,212 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC catheters recalled for lidocaine quality issue
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Groshong NXT catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC Provena catheters recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC SV catheters recalled for lidocaine defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC SOLO HF Catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard DuoGlide dialysis catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Poly Midline Catheter recalled for lidocaine manufacturing defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Access Systems drainage trays recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceCovidien LLCClass IINationwideCovidien Shiley decannulation plug recalled for mislabeled DEHP
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
- 2026-07-08FDA-DeviceCarl Zeiss MeditecClass IINationwideZeiss Intrabeam radiation applicator recalled for manufacturing defect
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono ceiling monitor recalled for loose screws
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the suspension may gradually loosen.
- 2026-07-08FDA-DeviceRaysearch LaboratoriesClass IINationwideRayCare 2024A SP4 recalled for beam delivery note data loss
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.
- 2026-07-08FDA-DeviceRaysearch LaboratoriesClass IINationwideRayCare 2024A SP1 recalled for beam note data loss risk
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.
- 2026-07-08FDA-DeviceMedela IncClass IIMedela ENFit ExSet extension set recalled for connector incompatibility
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
- 2026-07-08FDA-DeviceAccuray IncorporatedClass IINationwideAccuray Cyberknife recalled for collimator fall risk
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono floor recalled for movement capability loss
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono ceiling recalled for movement loss risk
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono biplane recalled for movement loss risk
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- 2026-07-08FDA-DeviceAccuray IncorporatedClass IINationwideAccuray Cyberknife recalled for collimator drop risk
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
- 2026-07-08FDA-DeviceTELEFLEX LLCClass IINationwidePilling Wecksorb Neurosponges recalled for endotoxin contamination
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
- 2026-07-08FDA-DeviceBaxterClass IINationwideBaxter operating table adapter recalled for loosening risk
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Section H V U component on Baxter operating tables.
- 2026-07-08FDA-DeviceBoston ScientificClass IINationwideBoston Scientific CRE Wireguided catheters recalled for sterile breach risk
Potential sterile breach of the pouches in which devices are packaged.
- 2026-07-08FDA-DeviceBoston ScientificClass IINationwideBoston Scientific CRE Wireguided catheters recalled for sterile breach risk
Potential sterile breach of the pouches in which devices are packaged.
- 2026-07-08FDA-DeviceBoston ScientificClass IINationwideBoston Scientific CRE Wireguided catheters recalled for sterile breach
Potential sterile breach of the pouches in which devices are packaged.
- 2026-07-08FDA-DeviceBoston ScientificClass IINationwideBoston Scientific CRE Wireguided catheter recalled for sterile breach risk
Potential sterile breach of the pouches in which devices are packaged.
- 2026-07-08FDA-DeviceBoston ScientificClass IINationwideCRE Wireguided 8-10mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
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